Total Knee Replacement Using Simplex® or Cobalt™ Bone Cement

Last updated: June 19, 2017
Sponsor: Zimmer Biomet
Overall Status: Trial Not Available

Phase

N/A

Condition

Rheumatoid Arthritis

Dermatomyositis (Connective Tissue Disease)

Osteoarthritis

Treatment

N/A

Clinical Study ID

NCT00589485
102-U-012
  • Ages > 18
  • All Genders

Study Summary

The purpose of this study is to collect radiographic and clinical outcomes of total knee replacement using Simplex® or Cobalt™ Bone Cement.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients with painful and disabled knee joint resulting from osteoarthritis,rheumatoid arthritis, traumatic arthritis where one or more compartments are involved

  • Patients requiring correction of varus, valgus, or posttraumatic deformity

  • Patients requiring correction or revision of unsuccessful osteotomy, arthrodesis, orfailure of previous joint replacement procedure

Exclusion

Exclusion Criteria:

  • Infection, sepsis, and osteomyelitis

Study Design

Study Start date:
November 01, 2006
Estimated Completion Date:
November 30, 2006

Study Description

The purpose of this study is to collect radiographic and clinical outcomes of total knee replacement using Simplex® or Cobalt™ Bone Cement.

Connect with a study center

  • Biomet Orthopedics, LLC

    Warsaw, Indiana 46581
    United States

    Site Not Available

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